Other mutations in this stock |
Total: 51 list
Gene | Ref | Var | Chr/Loc | Mutation | Predicted Effect | Zygosity |
Alad |
A |
G |
4: 62,511,922 (GRCm38) |
V121A |
probably damaging |
Het |
Anapc2 |
T |
A |
2: 25,284,676 (GRCm38) |
Y684N |
probably benign |
Het |
Arntl2 |
T |
C |
6: 146,820,590 (GRCm38) |
S220P |
probably damaging |
Het |
Atp10a |
G |
T |
7: 58,803,497 (GRCm38) |
R808L |
probably benign |
Het |
Best2 |
A |
G |
8: 85,009,354 (GRCm38) |
V317A |
probably damaging |
Het |
Cacnb4 |
A |
G |
2: 52,464,643 (GRCm38) |
L241P |
probably damaging |
Het |
Col6a5 |
T |
C |
9: 105,881,741 (GRCm38) |
T2089A |
possibly damaging |
Het |
Cttnbp2 |
G |
C |
6: 18,426,093 (GRCm38) |
A762G |
possibly damaging |
Het |
Defb13 |
G |
T |
8: 21,946,812 (GRCm38) |
V8F |
possibly damaging |
Het |
Dpp6 |
C |
T |
5: 26,817,810 (GRCm38) |
|
probably benign |
Het |
Fam126b |
A |
G |
1: 58,535,482 (GRCm38) |
V300A |
possibly damaging |
Het |
Fat4 |
A |
G |
3: 38,981,916 (GRCm38) |
D3239G |
possibly damaging |
Het |
Gm16486 |
C |
T |
8: 70,716,792 (GRCm38) |
S1177L |
probably benign |
Het |
Gm5615 |
A |
G |
9: 36,534,954 (GRCm38) |
V54A |
probably benign |
Het |
Hmcn1 |
T |
G |
1: 150,598,311 (GRCm38) |
R4793S |
possibly damaging |
Het |
Hspa1a |
T |
A |
17: 34,970,649 (GRCm38) |
Q426L |
probably damaging |
Het |
Il20rb |
T |
A |
9: 100,474,894 (GRCm38) |
Y61F |
probably damaging |
Het |
Itgb1 |
T |
A |
8: 128,722,401 (GRCm38) |
V496D |
possibly damaging |
Het |
Jakmip1 |
T |
C |
5: 37,159,765 (GRCm38) |
S102P |
unknown |
Het |
Jmjd8 |
T |
A |
17: 25,829,328 (GRCm38) |
F108I |
probably damaging |
Het |
Krtap15 |
A |
G |
16: 88,829,209 (GRCm38) |
T55A |
possibly damaging |
Het |
Lce3d |
A |
T |
3: 92,958,503 (GRCm38) |
|
probably benign |
Het |
Lnpep |
C |
A |
17: 17,546,499 (GRCm38) |
V702F |
probably damaging |
Het |
Lox |
G |
A |
18: 52,528,348 (GRCm38) |
A218V |
probably benign |
Het |
Mcrs1 |
T |
A |
15: 99,248,854 (GRCm38) |
K99* |
probably null |
Het |
Mfsd8 |
G |
A |
3: 40,846,835 (GRCm38) |
|
probably benign |
Het |
Msto1 |
G |
T |
3: 88,911,556 (GRCm38) |
P264Q |
probably damaging |
Het |
Nrp2 |
C |
T |
1: 62,745,408 (GRCm38) |
R239C |
probably damaging |
Het |
Olfr1002 |
G |
T |
2: 85,647,792 (GRCm38) |
H176Q |
probably damaging |
Het |
Olfr1368 |
T |
C |
13: 21,142,133 (GRCm38) |
D308G |
probably benign |
Het |
Pate2 |
A |
T |
9: 35,670,518 (GRCm38) |
H36L |
probably damaging |
Het |
Phf20l1 |
T |
G |
15: 66,639,948 (GRCm38) |
N925K |
possibly damaging |
Het |
Pnliprp2 |
G |
T |
19: 58,766,282 (GRCm38) |
V253F |
probably damaging |
Het |
Polr2b |
A |
G |
5: 77,336,506 (GRCm38) |
D745G |
probably damaging |
Het |
Ptdss1 |
T |
A |
13: 66,963,343 (GRCm38) |
W158R |
possibly damaging |
Het |
Rcn3 |
T |
A |
7: 45,084,907 (GRCm38) |
I226F |
probably damaging |
Het |
Rhbdl1 |
C |
G |
17: 25,835,851 (GRCm38) |
V157L |
probably damaging |
Het |
Slc30a2 |
A |
G |
4: 134,347,450 (GRCm38) |
T173A |
probably benign |
Het |
Spata16 |
A |
G |
3: 26,667,659 (GRCm38) |
T110A |
probably benign |
Het |
Specc1l |
A |
G |
10: 75,241,068 (GRCm38) |
K53E |
probably benign |
Het |
Speg |
G |
T |
1: 75,415,421 (GRCm38) |
|
probably benign |
Het |
Spta1 |
T |
A |
1: 174,240,171 (GRCm38) |
C2055S |
probably damaging |
Het |
Tex14 |
G |
A |
11: 87,509,600 (GRCm38) |
R406Q |
probably benign |
Het |
Tmem150b |
C |
T |
7: 4,716,328 (GRCm38) |
G198S |
probably null |
Het |
Tnfrsf14 |
T |
G |
4: 154,926,661 (GRCm38) |
Q81P |
probably damaging |
Het |
Txndc17 |
A |
G |
11: 72,207,742 (GRCm38) |
K40R |
probably benign |
Het |
Ube3a |
T |
A |
7: 59,284,756 (GRCm38) |
V560E |
probably damaging |
Het |
Vmn1r14 |
A |
G |
6: 57,234,030 (GRCm38) |
M198V |
probably damaging |
Het |
Vmn2r31 |
C |
T |
7: 7,384,200 (GRCm38) |
V791I |
probably damaging |
Het |
Wdfy4 |
T |
C |
14: 33,107,747 (GRCm38) |
Y984C |
|
Het |
Zfp386 |
T |
G |
12: 116,059,407 (GRCm38) |
D248E |
probably damaging |
Het |
|
Other mutations in Vmn2r23 |
Allele | Source | Chr | Coord | Type | Predicted Effect | PPH Score |
IGL00324:Vmn2r23
|
APN |
6 |
123,729,725 (GRCm38) |
missense |
possibly damaging |
0.89 |
IGL01012:Vmn2r23
|
APN |
6 |
123,729,596 (GRCm38) |
missense |
probably benign |
|
IGL01073:Vmn2r23
|
APN |
6 |
123,712,800 (GRCm38) |
missense |
possibly damaging |
0.82 |
IGL01547:Vmn2r23
|
APN |
6 |
123,704,424 (GRCm38) |
missense |
possibly damaging |
0.88 |
IGL01571:Vmn2r23
|
APN |
6 |
123,704,407 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL01950:Vmn2r23
|
APN |
6 |
123,741,886 (GRCm38) |
missense |
possibly damaging |
0.80 |
IGL02028:Vmn2r23
|
APN |
6 |
123,741,860 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02248:Vmn2r23
|
APN |
6 |
123,741,744 (GRCm38) |
missense |
probably damaging |
0.96 |
IGL02318:Vmn2r23
|
APN |
6 |
123,741,836 (GRCm38) |
missense |
probably benign |
0.10 |
IGL02649:Vmn2r23
|
APN |
6 |
123,704,478 (GRCm38) |
missense |
probably benign |
|
IGL02831:Vmn2r23
|
APN |
6 |
123,704,385 (GRCm38) |
missense |
probably benign |
0.22 |
IGL02832:Vmn2r23
|
APN |
6 |
123,704,396 (GRCm38) |
missense |
probably benign |
0.00 |
IGL02865:Vmn2r23
|
APN |
6 |
123,741,619 (GRCm38) |
missense |
probably damaging |
1.00 |
IGL02964:Vmn2r23
|
APN |
6 |
123,741,782 (GRCm38) |
missense |
possibly damaging |
0.93 |
IGL03347:Vmn2r23
|
APN |
6 |
123,704,374 (GRCm38) |
missense |
probably benign |
0.01 |
IGL03396:Vmn2r23
|
APN |
6 |
123,729,626 (GRCm38) |
missense |
probably damaging |
1.00 |
PIT4472001:Vmn2r23
|
UTSW |
6 |
123,712,977 (GRCm38) |
missense |
possibly damaging |
0.62 |
R0597:Vmn2r23
|
UTSW |
6 |
123,729,721 (GRCm38) |
missense |
probably benign |
0.08 |
R0677:Vmn2r23
|
UTSW |
6 |
123,713,451 (GRCm38) |
missense |
probably benign |
0.00 |
R0904:Vmn2r23
|
UTSW |
6 |
123,742,135 (GRCm38) |
missense |
probably damaging |
1.00 |
R1330:Vmn2r23
|
UTSW |
6 |
123,742,004 (GRCm38) |
missense |
probably damaging |
1.00 |
R1424:Vmn2r23
|
UTSW |
6 |
123,713,270 (GRCm38) |
nonsense |
probably null |
|
R1629:Vmn2r23
|
UTSW |
6 |
123,713,427 (GRCm38) |
missense |
probably benign |
0.05 |
R1842:Vmn2r23
|
UTSW |
6 |
123,729,690 (GRCm38) |
missense |
possibly damaging |
0.77 |
R1867:Vmn2r23
|
UTSW |
6 |
123,702,915 (GRCm38) |
missense |
probably damaging |
1.00 |
R1919:Vmn2r23
|
UTSW |
6 |
123,713,010 (GRCm38) |
missense |
possibly damaging |
0.94 |
R2087:Vmn2r23
|
UTSW |
6 |
123,741,499 (GRCm38) |
missense |
probably benign |
0.00 |
R2338:Vmn2r23
|
UTSW |
6 |
123,704,425 (GRCm38) |
missense |
possibly damaging |
0.88 |
R2568:Vmn2r23
|
UTSW |
6 |
123,742,188 (GRCm38) |
nonsense |
probably null |
|
R2867:Vmn2r23
|
UTSW |
6 |
123,713,164 (GRCm38) |
missense |
possibly damaging |
0.94 |
R2867:Vmn2r23
|
UTSW |
6 |
123,713,164 (GRCm38) |
missense |
possibly damaging |
0.94 |
R3500:Vmn2r23
|
UTSW |
6 |
123,713,170 (GRCm38) |
missense |
possibly damaging |
0.81 |
R3789:Vmn2r23
|
UTSW |
6 |
123,741,389 (GRCm38) |
missense |
probably damaging |
1.00 |
R4164:Vmn2r23
|
UTSW |
6 |
123,729,738 (GRCm38) |
missense |
probably benign |
|
R4506:Vmn2r23
|
UTSW |
6 |
123,702,925 (GRCm38) |
missense |
probably damaging |
1.00 |
R4652:Vmn2r23
|
UTSW |
6 |
123,741,730 (GRCm38) |
missense |
probably damaging |
1.00 |
R4697:Vmn2r23
|
UTSW |
6 |
123,741,826 (GRCm38) |
missense |
probably damaging |
1.00 |
R4840:Vmn2r23
|
UTSW |
6 |
123,713,074 (GRCm38) |
missense |
probably damaging |
1.00 |
R4983:Vmn2r23
|
UTSW |
6 |
123,733,349 (GRCm38) |
missense |
probably damaging |
1.00 |
R5276:Vmn2r23
|
UTSW |
6 |
123,712,977 (GRCm38) |
missense |
possibly damaging |
0.62 |
R5392:Vmn2r23
|
UTSW |
6 |
123,704,364 (GRCm38) |
missense |
probably benign |
0.36 |
R5528:Vmn2r23
|
UTSW |
6 |
123,713,002 (GRCm38) |
missense |
probably damaging |
1.00 |
R5529:Vmn2r23
|
UTSW |
6 |
123,713,451 (GRCm38) |
missense |
probably benign |
0.00 |
R5664:Vmn2r23
|
UTSW |
6 |
123,713,074 (GRCm38) |
missense |
probably damaging |
1.00 |
R5749:Vmn2r23
|
UTSW |
6 |
123,733,273 (GRCm38) |
missense |
probably benign |
|
R5761:Vmn2r23
|
UTSW |
6 |
123,712,759 (GRCm38) |
missense |
probably benign |
0.39 |
R5762:Vmn2r23
|
UTSW |
6 |
123,733,393 (GRCm38) |
missense |
probably damaging |
1.00 |
R5868:Vmn2r23
|
UTSW |
6 |
123,712,942 (GRCm38) |
missense |
probably benign |
0.12 |
R5935:Vmn2r23
|
UTSW |
6 |
123,741,895 (GRCm38) |
missense |
possibly damaging |
0.94 |
R6242:Vmn2r23
|
UTSW |
6 |
123,704,400 (GRCm38) |
missense |
possibly damaging |
0.82 |
R6416:Vmn2r23
|
UTSW |
6 |
123,712,902 (GRCm38) |
missense |
probably damaging |
1.00 |
R6524:Vmn2r23
|
UTSW |
6 |
123,713,425 (GRCm38) |
missense |
probably damaging |
1.00 |
R6576:Vmn2r23
|
UTSW |
6 |
123,733,273 (GRCm38) |
missense |
probably benign |
|
R6925:Vmn2r23
|
UTSW |
6 |
123,704,553 (GRCm38) |
missense |
probably damaging |
1.00 |
R7148:Vmn2r23
|
UTSW |
6 |
123,713,022 (GRCm38) |
missense |
probably benign |
|
R7215:Vmn2r23
|
UTSW |
6 |
123,704,364 (GRCm38) |
missense |
probably benign |
0.36 |
R7252:Vmn2r23
|
UTSW |
6 |
123,741,581 (GRCm38) |
missense |
probably damaging |
0.97 |
R7403:Vmn2r23
|
UTSW |
6 |
123,704,579 (GRCm38) |
missense |
probably benign |
0.01 |
R8143:Vmn2r23
|
UTSW |
6 |
123,741,353 (GRCm38) |
missense |
probably damaging |
0.99 |
R8474:Vmn2r23
|
UTSW |
6 |
123,704,640 (GRCm38) |
missense |
probably benign |
0.36 |
R8520:Vmn2r23
|
UTSW |
6 |
123,741,656 (GRCm38) |
missense |
probably damaging |
0.99 |
R8679:Vmn2r23
|
UTSW |
6 |
123,713,472 (GRCm38) |
missense |
probably damaging |
0.99 |
R8713:Vmn2r23
|
UTSW |
6 |
123,703,032 (GRCm38) |
missense |
|
|
R8966:Vmn2r23
|
UTSW |
6 |
123,742,120 (GRCm38) |
missense |
possibly damaging |
0.94 |
R9124:Vmn2r23
|
UTSW |
6 |
123,742,079 (GRCm38) |
missense |
possibly damaging |
0.57 |
R9163:Vmn2r23
|
UTSW |
6 |
123,741,823 (GRCm38) |
missense |
probably damaging |
1.00 |
R9189:Vmn2r23
|
UTSW |
6 |
123,704,364 (GRCm38) |
missense |
probably benign |
0.36 |
R9451:Vmn2r23
|
UTSW |
6 |
123,733,393 (GRCm38) |
missense |
probably damaging |
1.00 |
R9495:Vmn2r23
|
UTSW |
6 |
123,712,713 (GRCm38) |
missense |
probably benign |
0.30 |
R9514:Vmn2r23
|
UTSW |
6 |
123,712,713 (GRCm38) |
missense |
probably benign |
0.30 |
RF018:Vmn2r23
|
UTSW |
6 |
123,713,116 (GRCm38) |
missense |
probably benign |
0.00 |
T0975:Vmn2r23
|
UTSW |
6 |
123,713,161 (GRCm38) |
missense |
probably benign |
0.00 |
Z1088:Vmn2r23
|
UTSW |
6 |
123,742,108 (GRCm38) |
missense |
probably damaging |
0.98 |
Z1177:Vmn2r23
|
UTSW |
6 |
123,729,725 (GRCm38) |
frame shift |
probably null |
|
|